FDA.reportPublic FDA data

Menstrual Relief

Product NDC
50844-679
Requested package NDC
50844-679-27
11-digit product format
508440679
Labeler code
50844
Product ID
50844-679_098fa769-6439-46a8-b7c5-71a3457024b6
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen, Pamabrom, Pyrilamine maleate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
L.N.K. International, Inc.
Application
M027
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2015-01-13
Substance
ACETAMINOPHEN; PAMABROM; PYRILAMINE MALEATE
Active strength
500; 25; 15 mg/1; mg/1; mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Menstrual Relief
Brand name suffix
Maximum Strength
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1
PAMABROM25 mg/1
PYRILAMINE MALEATE15 mg/1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50844-679-27Menstrual ReliefMaximum Strength32 in 1 BOTTLETABLET, FILM COATED3213
50844-679-27Menstrual ReliefMaximum Strength1 in 1 CARTONTABLET, FILM COATED113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50844-679MENSTRUAL RELIEF MAXIMUM STRENGTH (ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]12Current NDC, Legacy NDC, 2 package rows20240829_92bb5cf5-5861-4f5e-91f7-9a546563c18e.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 3 · 43 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Midol CompleteACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATEBayer HealthCare LLC.ce9e6acb-a38b-4c9b-a7e8-3e1c2a49a3242025-04-10WarningsExact identifier
application number: M027
Diurex Water PillsCAFFEINE, MAGNESIUM SALICYLATEKobayashi Healthcare International, Inc.e02a39f9-1c8c-4d38-b394-3f5b7062932c2025-04-10WarningsExact identifier
application number: M027
Cramp TabsACETAMINOPHEN, PAMABROM, AND PYRILAMINE MALEATEJHK DBA American Safety & First Aidc090807d-03b7-42d4-be41-f6240a3b330f2024-10-04WarningsExact identifier
application number: M027

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1052637acetaminophen 500 MG / pamabrom 25 MG / pyrilamine maleate 15 MG Oral TabletPSN92bb5cf5-5861-4f5e-91f7-9a546563c18e13
1052637acetaminophen 500 MG / pamabrom 25 MG / pyrilamine maleate 15 MG Oral TabletSCD92bb5cf5-5861-4f5e-91f7-9a546563c18e13
1052637APAP 500 MG / pamabrom 25 MG / pyrilamine maleate 15 MG Oral TabletSY92bb5cf5-5861-4f5e-91f7-9a546563c18e13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50844-679-27508440679271 BOTTLE in 1 CARTON (50844-679-27) / 32 TABLET, FILM COATED in 1 BOTTLE1 bottle2015-01-130000-00-00NoNoCurrent